Table 1.
Study | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | MINORS score |
| |||||||||||||
Kim et al., 2005 [19] | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 1 | 2 | 0 | 2 | 21 |
Kwok et al., 2005 [25] | 2 | 1 | 2 | 2 | 2 | 2 | 2 | 2 | 0 | 2 | 2 | 2 | 21 |
Liu and Mori., 2005 [24] | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 1 | 2 | 0 | 2 | 21 |
Lee and Kim, 2010 [18] | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 1 | 2 | 0 | 2 | 21 |
Pournaras et al., 2011 [17] | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 0 | 2 | 0 | 2 | 20 |
Chang et al., 2013 [23] | 2 | 2 | 2 | 2 | 2 | 1 | 2 | 2 | 1 | 0 | 2 | 2 | 20 |
Oh et al., 2013 [16] | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 0 | 2 | 0 | 2 | 20 |
Ahn et al., 2014 [22] | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 1 | 2 | 0 | 2 | 21 |
(1) A stated aim of the study; (2) inclusion of consecutive patients; (3) prospective collection of data; (4) endpoints appropriate for the study aim; (5) unbiased evaluation of endpoints; (6) follow-up period appropriate to the major endpoint; (7) loss to follow-up not exceeding 5%; (8) a control group having the gold standard intervention; (9) contemporary groups; (10) baseline equivalence of groups; (11) prospective calculation of the sample size; (12) statistical analyses adapted to the study design.
0: not reported; 1: reported but inadequate; 2: reported and adequate.